Canonical Allele Identifier: CA403092032
Gene: MCOLN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7533773A>G , CM000681.2:g.7533773A>G GRCh38
NC_000019.9:g.7598659A>G , CM000681.1:g.7598659A>G GRCh37
NC_000019.8:g.7504659A>G NCBI36
NG_013374.1:g.4622A>G
NG_015806.1:g.16164A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.1721A>G MANE Select ENSP00000264079.5:p.Glu574Gly
ENST00000264079.10:c.1721A>G ENSP00000264079.5:p.Glu574Gly
ENST00000394321.9:n.2036A>G
ENST00000599334.1:c.449A>G
ENST00000601870.1:c.74A>G
ENST00000602227.1:n.275A>G
NM_020533.2:c.1721A>G NP_065394.1:p.Glu574Gly
NM_020533.3:c.1721A>G MANE Select NP_065394.1:p.Glu574Gly